Date published: 2026-5-21

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L-Valinol (CAS 2026-48-4)

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CAS Number:
2026-48-4
Molecular Weight:
103.16
Molecular Formula:
C5H13NO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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L-Valinol is an amino acid derivative that has been extensively studied for its biochemical effects. The specific mechanism of action of L-Valinol remains not fully understood, but it is believed to interact with various enzymes and receptors. Notably, L-Valinol may engage the G-protein coupled receptor, the serotonin receptor, and the GABA receptor. Additionally, it is thought to impact the activity of essential metabolic enzymes, such as fatty acid synthase, carnitine palmitoyltransferase, and acetyl-CoA carboxylase.


L-Valinol (CAS 2026-48-4) References

  1. Invariom-model refinement of L-valinol.  |  Dittrich, B., et al. 2006. Acta Crystallogr C. 62: o633-5. PMID: 17088630
  2. Quantification of structurally related aliphatic amino alcohols in l-valinol by hydrophilic interaction liquid chromatography separation combined with postcolumn derivatization and fluorescence detection.  |  Douša, M., et al. 2016. J Sep Sci. 39: 851-6. PMID: 26697727
  3. One-step multicomponent synthesis of chiral oxazolinyl-zinc complexes.  |  Luo, M., et al. 2017. Chem Cent J. 11: 81. PMID: 29086857
  4. [Rh(L-alaninate)(1,5-Cyclooctadiene)] Catalyzed Helix-Sense-Selective Polymerizations of Achiral Phenylacetylenes.  |  Wang, Q., et al. 2018. Polymers (Basel). 10: PMID: 30961148
  5. Translation in amino-acid-poor environments is limited by tRNAGln charging.  |  Pavlova, NN., et al. 2020. Elife. 9: PMID: 33289483
  6. Three-Component Aminoarylation of Electron-Rich Alkenes by Merging Photoredox with Nickel Catalysis.  |  Jiang, H., et al. 2021. Angew Chem Int Ed Engl. 60: 14399-14404. PMID: 33871137
  7. Enantio- and regioselective asymmetric allylic substitution using a chiral aminophosphinite ruthenium complex: an experimental and theoretical investigation.  |  Jena, RK. and Das, D. 2021. RSC Adv. 11: 39319-39327. PMID: 35492500
  8. Ribose conversion with amino acids into pyrraline platform chemicals - expeditious synthesis of diverse pyrrole-fused alkaloid compounds.  |  Cho, S., et al. 2021. RSC Adv. 11: 31511-31525. PMID: 35496880
  9. A Facile Synthesis of 2-Oxazolines via Dehydrative Cyclization Promoted by Triflic Acid.  |  Yang, T., et al. 2022. Molecules. 27: PMID: 36558175
  10. Jumping in the Chiral Pool: Asymmetric Hydroaminations with Early Metals.  |  Notz, S., et al. 2023. Molecules. 28: PMID: 36985673
  11. Rapid and Efficient Access to Novel Bio-Inspired 3-Dimensional Tricyclic SpiroLactams as Privileged Structures via Meyers' Lactamization.  |  Tangara, S., et al. 2023. Pharmaceuticals (Basel). 16: PMID: 36986512
  12. Atroposelective brominations to access chiral biaryl scaffolds using high-valent Pd-catalysis.  |  Linde, ST., et al. 2023. Chem Sci. 14: 3676-3681. PMID: 37006689
  13. Recent Developments in the Synthesis of HIV-1 Integrase Strand Transfer Inhibitors Incorporating Pyridine Moiety.  |  Starosotnikov, AM. and Bastrakov, MA. 2023. Int J Mol Sci. 24: PMID: 37298265

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-Valinol, 5 g

sc-295348
5 g
$42.00

L-Valinol, 25 g

sc-295348A
25 g
$136.00